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US 9,676,828 B2Granted
Rearranged TT virus molecules for use in diagnosis, prevention and treatment of cancer and autoimmunity
AssigneeDeutsches Krebsforschungszentrum
InventorsEthel-Michele De Villiers, Harald Zur Hausen
Life of this patent
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Abstract
The present invention relates to rearranged molecules of (a) a specific TT virus sequence and (b) a nucleotide sequence encoding a polypeptide showing homology to mammalian proteins associated with cancer and autoimmune diseases that are capable of replicating autonomously for use in diagnosis, prevention and treatment of diseases like cancer and autoimmunity.
Claims4
An expression vector comprising a rearranged torque teno virus (TTV) polynucleic acid comprising one of the nucleotide sequences of SEQ ID NOs:
- 228-231, wherein said nucleotide sequence is linked to a polynucleic acid encoding a polypeptide containing a signature motif of a mammalian protein being associated with cancer or an autoimmune disease, wherein the signature motif is at least 10 aa and has a degree of identity to a corresponding signature motif in a mammalian protein of at least 90% and said signature motif is selected from the group consisting of a protamine 1 signature motif having one of the sequences of SEQ ID NOs:17, 19, 22, and 241, a protamine 2 signature motif having one of the sequences of SEQ ID NOs:18, 20, 21, and 23, an opsin signature motif having one of the sequences of SEQ ID NOs:
- 1-16, and 36, a galanin signature motif having one of the SEQ ID NOs:26-28, a male specific protein signature motif having one of the SEQ ID NOs:53-54, a gastrin signature motif having one of the SEQ ID NOs:38-43, a collagen signature motif having one of the SEQ ID NOs:46-52, a collagenase metalloprotease signature motif having one of the SEQ ID NOs:44-45, a microbial collagenase metalloprotease (M9) signature motif having one of the SEQ ID NOs:55-60, a MIC1 microneme protein signature motif having one of the SEQ ID NOs:61-64:
- autoimmune regulator (AIRE) signature having one of the SEQ ID NOs:66-70, a gliadin signature motif having one of the SEQ ID NOs:72-77 and 155, a neuropeptide Y2 receptor signature motif having one of the SEQ ID NOs:79-81, an aerolysin signature motif having one of the SEQ ID NOs:83-87, an orexin signature motif having one of the SEQ ID NOs:89-95, a prion signature motif having one of the SEQ ID NOs:97-103, a neurotensin signature motif having one of the SEQ ID NOs:105-108, an orphan nuclear receptor (4A nuclear receptor) family signature motif having one of the SEQ ID NOs:110-117, a brain derived neurotrophic factor (BDN) signature motif having one of the SEQ ID NOs:118-119, a calcitonin signature motif having one of the SEQ ID NOs:121-128, a leukotrine B4 type 1 receptor signature motif having one of the SEQ ID NOs:129-135, a vasopressin signature motif having one of the SEQ ID NOs:136-147, a melanin concentrating hormone 2 receptor signature motif having one of the SEQ ID NOs:149-150, a prostanoid EP1 receptor signature motif having one of the SEQ ID NOs:152-154, a cyclin kinase signature motif having one of the SEQ ID NOs:158-169, a peroxisome proliferator-activated receptor signature motif having one of the SEQ ID NOs:171-178, a muscarinic M1 receptor signature motif having one of the SEQ ID NOs:180-184, a metabotropic gamma-aminobutyric acid type B2 receptor signature motif having one of the SEQ ID NOs:186-188, an argininge deiminase signature motif having one of the SEQ ID NOs:156 and 190-199, an opioid growth factor receptor repeat signature motif having the SEQ ID NO:201, an adhesion molecule CD36 signature motif having one of the SEQ ID NOs:203-209, a myelin proteolipid protein signature motif having the SEQ ID NO:211, and a chlamidiaom signature motif having the SEQ ID NO:213, wherein the rearranged TTV polynucleic acid is operably linked to prokaryotic, eukaryotic or viral transcription and translation control elements and comprising nucleic acid sequence providing expression of a desired open reading frame.
Dependencies are inferred from the claim text.